Canonical Allele Identifier: PA2826590542
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1915687
ClinVar RCV Id: RCV002594004
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Ser114Pro
CA2277304
NM_001281724.3:c.340T>C